WO2020259432A1 - Inhibiteur de kras-g12c - Google Patents

Inhibiteur de kras-g12c Download PDF

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Publication number
WO2020259432A1
WO2020259432A1 PCT/CN2020/097397 CN2020097397W WO2020259432A1 WO 2020259432 A1 WO2020259432 A1 WO 2020259432A1 CN 2020097397 W CN2020097397 W CN 2020097397W WO 2020259432 A1 WO2020259432 A1 WO 2020259432A1
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Prior art keywords
alkyl
substituted
halogen
compound
cycloalkyl
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PCT/CN2020/097397
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English (en)
Chinese (zh)
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谢雨礼
樊后兴
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微境生物医药科技(上海)有限公司
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Priority to CN202080016738.0A priority Critical patent/CN113544128B/zh
Publication of WO2020259432A1 publication Critical patent/WO2020259432A1/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Definitions

  • the present invention belongs to the field of medicinal chemistry, and more specifically, to a new type of KRAS-G12C inhibitor, its preparation method and the use method of the compound.
  • RAS represents a group of closely related monomeric globular proteins (21 kDa molecular weight), which have 189 amino acids and are connected to the plasma membrane and bind GDP or GTP. Under normal development or physiological conditions, RAS is activated by receiving growth factors and various other extracellular signals, and is responsible for regulating cell growth, survival, migration and differentiation. RAS acts as a molecular switch. The on/off state of the RAS protein is determined by nucleotide binding. The active signaling conformation is combined with GTP, and the inactive conformation is combined with GDP.
  • RAS When RAS contains bound GDP, it is in a dormant or resting or off state, and is "inactive", in response to exposure to certain growth-promoting stimuli, inducing RAS to convert bound GDP to GTP. As GTP is bound, RAS is "on” and can interact with and activate other proteins (its “downstream targets”).
  • the RAS protein itself has a very low inherent ability to hydrolyze GTP back to GDP and thereby turn itself into a closed state. The conversion of RAS to shutdown requires exogenous proteins called GTPase activating proteins (GAPs), which interact with RAS and greatly promote the conversion of GTP to GDP.
  • GAPs GTPase activating proteins
  • KRAS non-small cell lung cancer
  • KRAS mutations including G12C
  • other known driver oncogenic mutations in NSCLC including EGFR, ALK, ROS1, RET, and BRAF
  • KRAS mutations often co-occur with certain co-mutations, such as STK11, KEAP1, and TP53, which cooperate with mutant RAS to transform cells into highly malignant and aggressive tumor cells.
  • the present invention aims to provide a class of compounds with general structural formula as shown in formula (1), or each of its optical isomers, crystal forms, pharmaceutically acceptable salts, hydrates or solvates:
  • n 0, 1 or 2;
  • A is a bivalent 4-12 membered saturated or partially saturated monocyclic, bicyclic, bridged or spiro ring containing 1-2 N atoms.
  • the monocyclic, bicyclic, bridged or spiro ring may be optionally substituted by one substituted by one or more R 4, when a plurality of substituents R 4, R 4 may be the same or different;
  • Y is a chemical bond or C1-C6 alkylene group
  • R 1 is an aryl group or a heteroaryl group, and the aryl group or heteroaryl group can be substituted by 1-3 of the following groups: halogen, hydroxyl, amino, C1-C3 alkyl, C2-C4 alkenyl, C3 -C6 cycloalkyl, C1-C3 alkoxy, halogen substituted C1-C3 alkyl or halogen substituted C1-C3 alkoxy;
  • R 2 is an aminoalkyl group, a cycloalkyl group, an alkyl substituted amido group, a heterocyclic group, an aryl group or a heteroaryl group, and the heterocyclic group, aryl group or heteroaryl group may be optionally substituted by one or more R 5 , when it is substituted by multiple R 5 , R 5 may be the same or different;
  • R 3 independently selects C1-C3 alkyl or halo C1-C3 alkyl
  • R 4 is independently selected from H, CN, C1-C3 alkyl, halogen substituted C1-C3 alkyl, or cyano substituted C1-C3 alkyl;
  • R 5 is independently selected from halogen, H, O, CN, OH, alkylhydroxyl, dialkylamino, C1-C6 alkyl, C3-C6 cycloalkyl, halogen-substituted C1-C3 alkyl, or halogen-substituted C1- C3 alkoxy;
  • E is an electrophilic moiety capable of forming a covalent bond with the cysteine residue at position 12 of the K-Ras, H-Ras or N-Ras mutant protein.
  • E is a group containing an electrophilic carbon-carbon double bond or a carbon-carbon triple bond.
  • E is: Wherein, R a is H or F, R b is H, -CH 2 F, -CHF 2 ,
  • AE is: Wherein, n is 1 or 2, and R 4 is H, CN, C1-C3 alkyl, halogen substituted C1-C3 alkyl, or cyano substituted C1-C3 alkyl.
  • Y is a chemical bond, -CH 2 -, -CH(Me)- or -CH 2 CH 2 -.
  • R 1 is: Wherein R c and R d are independently halogen, hydroxyl, amino, C1-C3 alkyl, C2-C4 alkenyl, C3-C6 cycloalkyl, C1-C3 alkoxy, halogen substituted C1-C3 alkyl or halogen Substituted C1-C3 alkoxy.
  • R 2 is: Where n is 1 or 2, R e and R f are independently H, halogen, hydroxyl, amino, C1-C3 alkyl, C2-C4 alkenyl, C3-C6 cycloalkyl, C1-C3 alkoxy, halogen Substituted C1-C3 alkyl or halogen substituted C1-C3 alkoxy, R g is C1-C3 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylalkyl, C1-C3 alkoxyalkyl, Halogen substituted C1-C3 alkyl, halogen substituted C3-C6 cycloalkyl or
  • Another aspect of the present invention aims to provide a class of compounds whose general structural formula is represented by formula (2), or each of its optical isomers, crystal forms, pharmaceutically acceptable salts, hydrates or solvates :
  • A is a bivalent 4-12 membered saturated or partially saturated monocyclic, bicyclic, bridged or spiro ring containing 1-2 N atoms.
  • the monocyclic, bicyclic, bridged or spiro ring may be optionally substituted by one substituted by one or more R 4, when a plurality of substituents R 4, R 4 may be the same or different;
  • Y is a chemical bond or C1-C6 alkylene group
  • W is N, CR 8 or COR 6 :
  • R 2 is aminoalkyl, cycloalkyl, alkyl-substituted amido, heterocyclic, aryl or heteroaryl, the heterocyclic, aryl or heteroaryl group It may be optionally substituted by one or more R 5 , when it is substituted by more R 5 , R 5 may be the same or different;
  • R 2 is an aminoalkyl, alkyl substituted amido or heterocyclic group, and the heterocyclic group may be optionally substituted by one or more R 5 , when When one R 5 is substituted, R 5 may be the same or different;
  • R 1 is an aryl group or a heteroaryl group, and the aryl group or heteroaryl group can be substituted by 1-3 of the following groups: halogen, hydroxyl, amino, C1-C3 alkyl, C2-C4 alkenyl, C3 -C6 cycloalkyl, C1-C3 alkoxy, halogen substituted C1-C3 alkyl, halogen substituted C1-C3 alkoxy;
  • R 4 is independently selected from H, CN, C1-C3 alkyl, halogen substituted C1-C3 alkyl, or cyano substituted C1-C3 alkyl;
  • R 5 is independently selected from halogen, H, O, CN, OH, alkylhydroxyl, dialkylamino, C1-C6 alkyl, C3-C6 cycloalkyl, halogen substituted C1-C3 alkyl, or cyano substituted C1 -C3 alkyl;
  • R 6 is C1-C3 alkyl, halogen-substituted C1-C3 alkyl or C3-C6 cycloalkyl;
  • R 7 is H, halogen, C1-C3 alkyl, C3-C6 cycloalkyl, C1-C3 alkoxy, halogen substituted C1-C3 alkyl, halogen substituted C1-C3 alkoxy or C2-C4 alkenyl;
  • R 8 is H, halogen, C1-C3 alkyl, C3-C6 cycloalkyl, or halogen substituted C1-C3 alkyl;
  • E is an electrophilic moiety capable of forming a covalent bond with the cysteine residue at position 12 of the K-Ras, H-Ras or N-Ras mutant protein.
  • E is a group containing an electrophilic carbon-carbon double bond or a carbon-carbon triple bond.
  • E is: Wherein, R a is H or F, R b is H, -CH 2 F, -CHF 2 ,
  • AE is: Wherein, n is 1 or 2, wherein R 4 is H, CN, C1-C3 alkyl, halogen substituted C1-C3 alkyl, or cyano substituted C1-C3 alkyl.
  • Y is a chemical bond, -CH 2 -, -CH(Me)- or -CH 2 -CH 2 -.
  • R 1 is: Wherein R c and R d are independently halogen, hydroxy, amino, C1-C3 alkyl, C2-C4 alkenyl, C3-C6 cycloalkyl, C1-C3 alkoxy, halogen-substituted C1-C3 alkyl or halogen Substituted C1-C3 alkoxy.
  • W is COR 6 and R 2 is:
  • R e and R f are independently halogen, hydroxy, amino, C1-C3 alkyl, C2-C4 alkenyl, C3-C6 cycloalkyl, C1-C3 alkoxy, halogen substituted C1 -C3 alkyl or halogen substituted C1-C3 alkoxy
  • R g is C1-C3 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylalkyl, C1-C3 alkoxyalkyl, halogen Substituted C1-C3 alkyl, halogen substituted C3-C6 cycloalkyl or
  • W is N or CR 8
  • R 2 is: Where n is 1 or 2, R e and R f are independently halogen, hydroxy, amino, C1-C3 alkyl, C2-C4 alkenyl, C3-C6 cycloalkyl, C1-C3 alkoxy, halogen substituted C1 -C3 alkyl or halogen substituted C1-C3 alkoxy, R g is C1-C3 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkylalkyl, C1-C3 alkoxyalkyl, halogen substituted C1-C3 alkyl, halogen substituted C3-C6 cycloalkyl or
  • the compound has one of the structures listed in Table 1 below:
  • Another object of the present invention is to provide a pharmaceutical composition, which contains a pharmacologically acceptable excipient or carrier, and the compound of the general formula (1) or general formula (2) of the present invention, or their respective optical differences Constructs, pharmaceutically acceptable inorganic or organic salts are used as active ingredients.
  • Another object of the present invention is to provide the use of the above-mentioned compound of the present invention, or each of its optical isomers, or pharmaceutically acceptable inorganic or organic salts, for preparing and treating tumor-related diseases.
  • the compounds of the general formula (1) and (2) described above can be synthesized using standard synthesis techniques or well-known techniques and methods combined in the text. In addition, the solvent, temperature and other reaction conditions mentioned here can be changed.
  • the starting materials for the synthesis of the compound can be synthesized or obtained from commercial sources such as, but not limited to, Aldrich Chemical Co. (Milwaukee, Wis.) or Sigma Chemical Co. (St. Louis, Mo.).
  • the compounds described herein and other related compounds with different substituents can be synthesized using well-known techniques and raw materials, including those found in March, ADVANCED ORGANIC CHEMISTRY 4 th Ed., (Wiley 1992); Carey and Sundberg, ADVANCED ORGANIC CHEMISTRY 4 th Ed., Vols. A and B (Plenum 2000, 2001), Green and Wuts, PROTECTIVE GROUPS IN ORGANIC SYNTHESIS 3 rd Ed., (Wiley 1999).
  • the general method of compound preparation can be changed by using appropriate reagents and conditions for introducing different groups in the molecular formula provided herein.
  • the compounds described herein are according to methods well known in the art.
  • the conditions of the method such as reactants, solvents, bases, amounts of compounds used, reaction temperature, time required for the reaction, etc. are not limited to the following explanations.
  • the compounds of the present invention can also be conveniently prepared by combining various synthetic methods described in this specification or known in the art, and such combinations can be easily performed by those skilled in the art to which the present invention belongs.
  • the present invention also provides a method for preparing the compound represented by the general formula (1) and the general formula (2), which is prepared by the following general reaction schemes 1, 2, 3 or 4:
  • the embodiment of the compound of general formula (1) can be prepared according to general reaction scheme 1 (method A), wherein R 1 , R 2 , R 4 , A, E and Y are as defined above, and X represents I, Br, Cl, OTf , -B(OH) 2 and other groups.
  • general reaction scheme 1 the intermediate A1 (synthesized according to the method described in WO2017201161) and the fragment A produce A2 under alkaline conditions
  • the compound of structure A2 produces A3 in the presence of an oxidizing agent
  • the compound A3 produces A4 under alkaline conditions.
  • A4 reacts with R 2 -YX fragments under appropriate conditions to produce A5, A5 removes the protective group (such as Boc) to obtain A6, A6 and R1-X couple to obtain A7, A7 removes the protective group (such as Cbz) to obtain A8 , A8 reacts with acid chloride or acid anhydride compound to generate A9.
  • A5 removes the protective group (such as Boc) to obtain A6, A6 and R1-X couple to obtain A7, A7 removes the protective group (such as Cbz) to obtain A8 , A8 reacts with acid chloride or acid anhydride compound to generate A9.
  • the embodiment of the compound of general formula (2) can be prepared according to general reaction scheme 2 (method B), wherein R 1 , R 2 , R 4 , R 6 , R 7 , A, E and Y are as defined above, X represents groups such as I, Br, Cl, OTf, -B(OH) 2 and the like.
  • intermediate B1 (synthesized with reference to the method described in WO2016164675) and fragment A generate B2 under basic conditions
  • compound B2 under basic conditions produces B3, and compound B3 under basic conditions B4, B4 react with R 2 -YX fragments under appropriate conditions to generate B5, B5 and R 1 -X are coupled to obtain B6, B6 continues to be coupled with R 7 X to obtain B7, and B7 is obtained by removing the protective group (such as Cbz) B8, B8 and acid chloride or acid anhydride compound react to produce B9.
  • protective group such as Cbz
  • the embodiment of the compound of general formula (2) can be prepared according to General Reaction Scheme 3 (Method C), wherein R 1 , R 2 , R 4 , R 7 , A, E and Y are as defined above, and X represents I, Br, Cl, OTf, -B(OH) 2 and other groups.
  • the intermediate C1 (synthesized with reference to the method described in US2016164675) undergoes amidation reaction to generate C2, the structure C2 compound reacts with an appropriate reagent to generate substituted isocyanate, which further reacts to generate C3, and compound C3 is basic Under appropriate conditions, the reaction produces pyrimidinedione intermediate C4, C4 reacts with chlorinating reagents under appropriate conditions to produce C5, C5 reacts under alkaline conditions to produce C6, C6 and R 1 -X are coupled to obtain C7, C7 deprotection group ( For example, Boc) obtains C8, C8 reacts with acid chloride or acid anhydride compound to generate C9.
  • Boc Boc
  • the embodiment of the compound of general formula (2) can be prepared according to general reaction scheme 4 (method D), wherein R 1 , R 2 , R 4 , R 7 , R 8 , A, E and Y are as defined above .
  • general reaction scheme 4 intermediate D1 (synthesized with reference to the method described in WO2016164675) and fragment A generate D2 under alkaline conditions, and the compound of structure D2 generates D3 under alkaline conditions, and D3 and R 2 under appropriate conditions -YX fragments react to form D4, D4 and R 1 -X are coupled to form D5, D5 is deprotected (such as Boc) to form D6, and D6 is reacted with acid chloride or acid anhydride compound to form D7.
  • D5 is deprotected (such as Boc) to form D6
  • D6 is reacted with acid chloride or acid anhydride compound to form D7.
  • “Pharmaceutically acceptable” here refers to a substance, such as a carrier or diluent, that does not make the biological activity or properties of the compound disappear, and is relatively non-toxic, for example, when a substance is administered to an individual, it does not cause unwanted biological effects or Interacts with any components it contains in a harmful way.
  • pharmaceutically acceptable salt refers to a form of a compound that does not cause important irritation to the administered organism and does not cause the biological activity and properties of the compound to disappear.
  • pharmaceutically acceptable salts are obtained by reacting compounds of formula (1) or formula (2) with acids, such as inorganic acids such as hydrochloric acid, hydrobromic acid, hydrofluoric acid, sulfuric acid, phosphoric acid, nitric acid, phosphoric acid, etc.
  • references to pharmaceutically acceptable salts include solvent addition forms or crystalline forms, especially solvates or polymorphs.
  • Solvates contain stoichiometric or non-stoichiometric solvents, and are selectively formed during crystallization with pharmaceutically acceptable solvents such as water, ethanol, etc.
  • a hydrate is formed when the solvent is water, or an alcoholate is formed when the solvent is ethanol.
  • the solvate of the compound of formula (1) or formula (2) is conveniently prepared or formed according to the method described herein.
  • the hydrate of the compound of formula (1) or formula (2) is conveniently prepared by recrystallization from a mixed solvent of water/organic solvent.
  • the organic solvents used include, but are not limited to, dioxane and tetrahydrofuran. , Ethanol or methanol.
  • the compounds mentioned here can exist in unsolvated and solvated forms. In summary, for the purposes of the compounds and methods provided herein, the solvated form is considered equivalent to the unsolvated form.
  • the compounds of formula (1) or (2) are prepared in different forms, including, but not limited to, amorphous, pulverized, and nano-particle size forms.
  • the compound of formula (1) or formula (2) includes a crystalline form, and may also be a polymorphic form.
  • Polymorphs include different lattice arrangements of the same elemental composition of the compound. Polymorphs usually have different X-ray diffraction patterns, infrared spectra, melting points, density, hardness, crystal form, optical and electrical properties, stability and solubility. Different factors such as recrystallization solvent, crystallization rate and storage temperature may cause a single crystal form to dominate.
  • the compound of formula (1) or formula (2) has one or more stereocenters, and is therefore classified as racemate, racemic mixture, single enantiomer, diastereomeric compound and single diastereomer Appears in the form of enantiomers.
  • the asymmetric centers that can exist depend on the nature of the various substituents on the molecule. Each such asymmetric center will independently produce two optical isomers, and all possible mixtures of optical isomers and diastereomers and pure or partially pure compounds are included in the scope of the present invention. The present invention is meant to include all such isomeric forms of these compounds.
  • Alkyl refers to saturated aliphatic hydrocarbon groups, including straight and branched chain groups of 1 to 6 carbon atoms. Preferably, a lower alkyl group containing 1 to 4 carbon atoms, such as methyl, ethyl, propyl, 2-propyl, n-butyl, isobutyl, tert-butyl.
  • alkyl includes unsubstituted and substituted alkyl groups, especially alkyl groups substituted with one or more halogens.
  • Preferred alkyl groups are selected from CH 3 , CH 3 CH 2 , CF 3 , CHF 2 , CF 3 CH 2 , i Pr, n Pr, i Bu, c Pr, n Bu or t Bu.
  • Cycloalkyl refers to a 3- to 6-membered all-carbon monocyclic aliphatic hydrocarbon group, in which one or more rings may contain one or more double bonds, but none of the rings have a fully conjugated ⁇ -electron system.
  • cyclopropyl, cyclobutyl, cyclopentyl, cyclohexane, cyclohexadiene and the like are examples of the rings.
  • Alkoxy refers to an alkyl group bonded to the rest of the molecule through an ether oxygen atom.
  • Representative alkoxy groups are those with 1-6 carbon atoms, such as methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, sec-butoxy And tert-butoxy.
  • alkoxy includes unsubstituted and substituted alkoxy, especially alkoxy substituted with one or more halogens.
  • Preferred alkoxy groups are selected from OCH 3 , OCF 3 , CHF 2 O, CF 3 CH 2 O, i PrO, n PrO, i BuO, c PrO, n BuO or t BuO.
  • Aryl refers to a group having at least one aromatic ring structure, that is, a carbocyclic aryl group having a conjugated ⁇ electron system, such as a benzene ring and a naphthalene ring.
  • Heteroaryl refers to an aromatic group containing one or more heteroatoms (O, S or N).
  • the heteroaryl group is monocyclic or polycyclic, such as a monocyclic heteroaryl ring and one or more carbocyclic rings. Aromatic groups or other monocyclic heterocyclic groups are condensed.
  • heteroaryl groups include, but are not limited to, pyridyl, pyridazinyl, imidazolyl, pyrimidinyl, pyrazolyl, triazolyl, pyrazinyl, quinolinyl, isoquinolinyl, tetrazolyl, furanyl , Thienyl, isoxazolyl, thiazolyl, oxazolyl, isothiazolyl, pyrrolyl, indolyl, benzimidazolyl, benzofuranyl, benzothiazolyl, benzothienyl, benzoxanyl Azolyl, benzopyridyl and pyrrolopyrimidinyl.
  • Halogen refers to fluorine, chlorine, bromine or iodine.
  • bond refers to a chemical bond between two atoms or between two fragments (when the atoms connected by a bond are considered part of a larger structure).
  • bond refers to a chemical bond between two atoms or between two fragments (when the atoms connected by a bond are considered part of a larger structure).
  • bond when the group described herein is a bond, the lack of a reference group allows a bond to be formed between the remaining defined groups.
  • membered ring includes any cyclic structure.
  • element means to indicate the number of skeletal atoms constituting the ring.
  • cyclohexyl, pyridyl, pyranyl, and thiopyranyl are six-membered rings
  • cyclopentyl, pyrrolyl, furyl, and thienyl are five-membered rings.
  • fragment refers to a specific part or functional group of a molecule. Chemical fragments are generally considered to be chemical entities contained or attached to molecules.
  • treatment refers to a prescription component or active ingredient that does not have unduly harmful effects on the health of the general treatment target.
  • treatment includes alleviating, inhibiting, or improving the symptoms or conditions of diseases; inhibiting the occurrence of complications; improving or preventing underlying metabolic syndrome; inhibiting the occurrence of diseases or symptoms, Such as controlling the development of diseases or conditions; reducing diseases or symptoms; reducing diseases or symptoms; reducing complications caused by diseases or symptoms, or preventing or treating signs caused by diseases or symptoms.
  • a certain compound or pharmaceutical composition after administration, can improve a certain disease, symptom or condition, especially its severity, delay the onset, slow the progression of the disease, or reduce the duration of the disease. Regardless of fixed administration or temporary administration, continuous administration or intermittent administration, it can be attributed to or related to the administration.
  • Active ingredient refers to a compound represented by general formula (1) or general formula (2), and a pharmaceutically acceptable inorganic or organic salt of a compound of general formula (1) or general formula (2).
  • the compounds of the present invention may contain one or more asymmetric centers, and therefore appear as racemates, racemic mixtures, single enantiomers, diastereomeric compounds, and single diastereomers.
  • the asymmetric centers that can exist depend on the nature of the various substituents on the molecule. Each such asymmetric center will independently produce two optical isomers, and all possible mixtures of optical isomers and diastereomers and pure or partially pure compounds are included within the scope of the present invention.
  • the present invention is meant to include all such isomeric forms of these compounds.
  • composition refers to when applied to an individual (human Or animal), a compound or composition that can induce the desired pharmaceutical and/or physiological response through local and/or systemic effects.
  • administered refers to the direct administration of the compound or composition, or the administration of a prodrug, derivative, or analog of the active compound Etc., and can form an equivalent amount of the active compound in the subject of administration.
  • the present invention provides methods for using the compounds or pharmaceutical compositions of the present invention to treat conditions, including but not limited to conditions involving G12C K-Ras, G12C H-Ras, and/or G12C N-Ras mutations (such as cancer).
  • a method for cancer treatment comprising administering to an individual in need an effective amount of any of the aforementioned pharmaceutical compositions comprising a compound of structure (1) or (2).
  • the cancer is mediated by K-Ras, H-Ras, and/or G12C N-Ras mutations.
  • the cancer is lung cancer, pancreatic cancer, colon cancer, MYH-related polyposis, or colorectal cancer.
  • the compound of the present invention and its pharmaceutically acceptable salt can be prepared into various preparations, which contain a safe and effective amount of the compound of the present invention or its pharmaceutically acceptable salt and a pharmacologically acceptable excipient or carrier .
  • the "safe and effective amount” refers to: the amount of the compound is sufficient to significantly improve the condition without causing serious side effects.
  • the safe and effective amount of the compound is determined according to the age, condition, and course of treatment of the subject to be treated.
  • “Pharmaceutically acceptable excipient or carrier” refers to: one or more compatible solid or liquid fillers or gel substances, which are suitable for human use, and must have sufficient purity and sufficiently low toxicity .
  • Compatibility here means that each component of the composition can be blended with the compound of the present invention and between them without significantly reducing the efficacy of the compound.
  • pharmacologically acceptable excipients or carriers include cellulose and its derivatives (such as sodium carboxymethyl cellulose, sodium ethyl cellulose, cellulose acetate, etc.), gelatin, talc, solid lubricants (such as stearic acid, magnesium stearate), calcium sulfate, vegetable oils (such as soybean oil, sesame oil, peanut oil, olive oil, etc.), polyols (such as propylene glycol, glycerin, mannitol, sorbitol, etc.), emulsifiers Wetting agents (such as sodium lauryl sulfate), coloring agents, flavoring agents, stabilizers, antioxidants, preservatives, pyrogen-free water, etc.
  • cellulose and its derivatives such as sodium carboxymethyl cellulose, sodium ethyl cellulose, cellulose
  • Solid dosage forms for oral administration include capsules, tablets, pills, powders and granules.
  • the active compound is mixed with at least one conventional inert excipient (or carrier), such as sodium citrate or dicalcium phosphate, or mixed with the following ingredients: (a) fillers or compatibilizers, for example, Starch, lactose, sucrose, glucose, mannitol and silicic acid; (b) binders such as hydroxymethyl cellulose, alginate, gelatin, polyvinylpyrrolidone, sucrose and gum arabic; (c) humectants, For example, glycerin; (d) disintegrants, such as agar, calcium carbonate, potato starch or tapioca starch, alginic acid, certain complex silicates, and sodium carbonate; (e) slow solvents, such as paraffin; (f) Absorption accelerators, such as quaternary amine compounds; (g) wetting agents, such as cetyl alcohol and glycty
  • Solid dosage forms such as tablets, sugar pills, capsules, pills and granules can be prepared with coatings and shell materials, such as enteric coatings and other materials known in the art. They may contain opacifying agents, and the active compound or the release of the compound in such a composition may be released in a certain part of the digestive tract in a delayed manner. Examples of embedding components that can be used are polymeric substances and waxes. If necessary, the active compound can also be formed into microcapsules with one or more of the above-mentioned excipients.
  • Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, solutions, suspensions, syrups or tinctures.
  • the liquid dosage form may contain inert diluents conventionally used in the art, such as water or other solvents, solubilizers and emulsifiers, for example, ethanol, isopropanol, ethyl carbonate, ethyl acetate, propylene glycol, 1 , 3-Butanediol, dimethylformamide and oils, especially cottonseed oil, peanut oil, corn germ oil, olive oil, castor oil and sesame oil or mixtures of these substances.
  • the composition may also contain adjuvants such as wetting agents, emulsifying and suspending agents, sweetening agents, flavoring agents and perfumes.
  • the suspension may contain suspending agents, for example, ethoxylated isostearyl alcohol, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum methoxide and agar, or mixtures of these substances, and the like.
  • composition for parenteral injection may contain physiologically acceptable sterile aqueous or non-aqueous solutions, dispersions, suspensions or emulsions, and sterile powders for reconstitution into sterile injectable solutions or dispersions.
  • Suitable aqueous and non-aqueous carriers, diluents, solvents or excipients include water, ethanol, polyols and suitable mixtures thereof.
  • the dosage form of the compound of the present invention for topical administration includes ointment, powder, patch, spray and inhalant.
  • the active ingredient is mixed under sterile conditions with a physiologically acceptable carrier and any preservatives, buffers, or propellants that may be required if necessary.
  • the compound of the present invention can be administered alone or in combination with other pharmaceutically acceptable compounds.
  • a safe and effective amount of the compound of the present invention is applied to a mammal (such as a human) in need of treatment, wherein the dosage is the pharmaceutically effective dosage considered to be administered.
  • the daily administration dose is usually 1 to 1000 mg, preferably 10 to 500 mg.
  • the specific dosage should also consider factors such as the route of administration, the patient's health status, etc., which are within the skill range of a skilled physician.
  • Ar stands for argon; CDCl 3 stands for deuterated chloroform; CDI stands for 1,1'-carbonyldiimidazole; CD 3 OD stands for deuterated methanol; CuI stands for cuprous iodide; Methyl chloride; DIPEA stands for diisopropylethylamine; DMF stands for dimethylformamide; DMSO stands for dimethyl sulfonate; EA stands for ethyl acetate; h stands for hours; NaOH stands for sodium hydroxide; LC-MS stands for liquid Phase-mass spectrometry; m-CPBA stands for m-chloroperoxybenzoic acid; MeOH stands for methanol; min stands for minutes; MS stands for mass spectrometry; NMR stands for nuclear magnetic resonance; Pd(dppf)2Cl2 stands for [1,1'-bis(diphenylphosphine) ) Ferrocene] dichloropalladium dichloropalladium dichloro
  • Compound 1 was prepared according to Method A as described below:
  • Compound 53 was prepared according to Method B as described below:
  • CDI (35.6g, 220mmol) was added to C1 (42g, 200mmol) in THF (400mL) in batches. The mixture was stirred for 5min, protected by Ar, heated to 50°C, reacted for 1h, monitored by LC-MS, and the raw materials disappeared. The solution was diluted with toluene (100 mL) and concentrated to half of the initial volume. The resulting mixture was cooled to 0° C., and ammonium hydroxide (55 mL, 400 mmol) was slowly added. React at room temperature for 10 minutes, dilute with EA (200 mL), and wash with water (100 mL*3). The organic layer was dried with anhydrous Na 2 SO 4 and spin-dried.
  • H358 cells were planted in an ultra-low adsorption six-well plate. After one day of growth, the compound to be tested (at a concentration of 1 ⁇ M) was added. After the compound was used for 24 hours, the cells were lysed, and GST-Raf1(1-149) was added ( millipore 14-863), after incubating at 4°C overnight, add GST beads (millipore, G0924), incubate at 4°C for 2 hours, then centrifuge, take the beads, wash the beads with IP buffer 3 times, then add SDS lysis solution, and run Gel, use Ras antibody (CST, 3339) western blot to detect the pulled Ras-GTP content. Compared with the DMSO group, the percentage of the compound inhibiting Ras-GTP activity was calculated. The results are shown in Table 2 below.
  • Compound Inhibition rate(%) Compound Inhibition rate(%) Compound Inhibition rate(%) 1 +++ 2 ++ 3 ++ 4 ++ 5 ++ 6 ++ 7 ++ 8 + 9 ++ 10 +++ 11 +++ 12 +++ 13 +++ 14 +++ 15 +++ 16 +++ 17 +++ 18 +++ 19 +++ 20 ++ twenty one +++ twenty two +++ twenty three +++ twenty four +++
  • +++ means the inhibition rate is greater than 90%
  • Compound Inhibition rate(%) Compound Inhibition rate(%) Compound Inhibition rate(%) 1 +++ 2 ++ 3 ++ 4 + 5 ++ 6 ++ 7 ++ 8 + 9 ++ 10 +++ 11 +++ 12 +++ 13 +++ 14 +++ 15 +++ 16 +++ 17 +++ 18 +++ 19 ++ 20 +++ twenty one +++ twenty two +++ twenty three +++ twenty four +++ 25 +++ 26 +++ 27 +++ 28 +++ 29 +++ 30 ++ 31 +++ 32 +++ 33 +++ 34 +++ 35 +++ 36 +++ 37 ++ 38 +++ 39 +++ 40 +++ 41 +++ 42 +++ 43 +++ 44 +++ 45 +++ 46 +++ 47 +++ 48 +++ 49 +++ 50 +++ 51 ++ 52 ++ 53 +++ 54 +++ 55 +++ 56 +++ 57 +++ 58 +++ 59 ++ 60 +++ 61 +++ 62 +++ 63 +++
  • +++ means the inhibition rate is less than 1 ⁇ M
  • the compounds of the present invention have good biological activities, including the inhibitory activity of Ras-GTP in H358 cells and the anti-proliferation activity of H358 cells.

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Abstract

La présente invention concerne un inhibiteur irréversible de la protéine K-Ras mutante G12C. L'invention concerne également l'inhibiteur irréversible de la protéine K-Ras mutante G12C ainsi que son procédé de préparation et son utilisation.
PCT/CN2020/097397 2019-06-26 2020-06-22 Inhibiteur de kras-g12c WO2020259432A1 (fr)

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WO2022060583A1 (fr) 2020-09-03 2022-03-24 Revolution Medicines, Inc. Utilisation d'inhibiteurs de sos1 pour traiter des malignités à mutations de shp2
WO2022222871A1 (fr) * 2021-04-21 2022-10-27 Beijing Innocare Pharma Tech Co., Ltd. Composés hétérocycliques en tant qu'inhibiteurs de kras g12c
WO2022266206A1 (fr) 2021-06-16 2022-12-22 Erasca, Inc. Conjugués d'inhibiteurs de kras
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WO2024206858A1 (fr) 2023-03-30 2024-10-03 Revolution Medicines, Inc. Compositions pour induire une hydrolyse de ras gtp et leurs utilisations
US12122787B2 (en) 2019-09-20 2024-10-22 Shanghai Jemincare Pharmaceuticals Co., Ltd Fused pyridone compound, and preparation method therefor and use thereof

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CN112047937B (zh) * 2019-06-06 2023-04-07 劲方医药科技(上海)有限公司 四氢吡啶并[3,4-d]嘧啶-2(1H)-酮类化合物，其制法与医药上的用途
CN110256421A (zh) * 2019-06-26 2019-09-20 微境生物医药科技(上海)有限公司 Kras-g12c抑制剂
CN112574224A (zh) * 2019-09-30 2021-03-30 上海迪诺医药科技有限公司 Kras g12c抑制剂及其应用
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CN113045565A (zh) * 2019-12-27 2021-06-29 微境生物医药科技(上海)有限公司 新型K-Ras G12C抑制剂
CN112094269B (zh) * 2020-01-01 2021-12-07 上海凌达生物医药有限公司 一类饱和六元环并杂环类化合物、制备方法和用途
CN113637005B (zh) * 2020-02-24 2024-05-24 泰励生物科技（上海）有限公司 用于癌症治疗的kras抑制剂
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Cited By (11)

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Publication number Priority date Publication date Assignee Title
US12065430B2 (en) 2018-10-26 2024-08-20 Taiho Pharmaceutical Co., Ltd. Indazole compound or salt thereof
US12122787B2 (en) 2019-09-20 2024-10-22 Shanghai Jemincare Pharmaceuticals Co., Ltd Fused pyridone compound, and preparation method therefor and use thereof
US11697657B2 (en) 2019-10-28 2023-07-11 Merck Sharp & Dohme Llc Small molecule inhibitors of KRAS G12C mutant
WO2021257736A1 (fr) 2020-06-18 2021-12-23 Revolution Medicines, Inc. Méthodes de retardement, de prévention et de traitement de la résistance acquise aux inhibiteurs de ras
WO2022060583A1 (fr) 2020-09-03 2022-03-24 Revolution Medicines, Inc. Utilisation d'inhibiteurs de sos1 pour traiter des malignités à mutations de shp2
WO2022222871A1 (fr) * 2021-04-21 2022-10-27 Beijing Innocare Pharma Tech Co., Ltd. Composés hétérocycliques en tant qu'inhibiteurs de kras g12c
WO2022266206A1 (fr) 2021-06-16 2022-12-22 Erasca, Inc. Conjugués d'inhibiteurs de kras
WO2023031781A1 (fr) 2021-09-01 2023-03-09 Novartis Ag Combinaisons pharmaceutiques comprenant un inhibiteur de tead et leurs utilisations pour le traitement de cancers
WO2024081674A1 (fr) 2022-10-11 2024-04-18 Aadi Bioscience, Inc. Polythérapies pour le traitement du cancer
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WO2024206858A1 (fr) 2023-03-30 2024-10-03 Revolution Medicines, Inc. Compositions pour induire une hydrolyse de ras gtp et leurs utilisations

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